About this opportunity
Implant Direct lists this Global Medical Device Regulatory Affairs Specialist opportunity in thousand oaks, California. Review the employer’s description below for duties, qualifications and application requirements.
Job description
Implant Direct in Thousand Oaks, CA is seeking a Regulatory Affairs Specialist to manage global regulatory submissions for medical devices, including US 510(k), EU technical documentation, and international dossiers.
The role represents Regulatory Affairs on cross-functional teams, provides regulatory strategy, assesses impact of design changes, and ensures ongoing compliance across markets while supporting audits and regulatory developments.
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Worksite address
thousand oaks, CA, 91362, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.